A High Performance Liquid Chromatography (HPLC) method utilizing fluorescence detection was developed in our laboratory. We evaluated the pharmacokinetics and dose proportionality of Tacrine(registered trademark) after oral doses of 10 mg and 20 mg. Serial blood sampling was carried out after dosing over a twelve hour period. We also attempted to correlate plasma concentration with both cognitive improvement and adverse effects.

Agency
National Institute of Health (NIH)
Institute
Clinical Center (CLC)
Type
Intramural Research (Z01)
Project #
1Z01CL005055-02
Application #
3896270
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Clinical Center
Department
Type
DUNS #
City
State
Country
United States
Zip Code